Global Regulatory Projects Lead – GRAPS Enablement

Ascendis Pharma; Hellerup; On-site; DKK 1,100,000 - 1,400,000; Full time

Benefits offered by this job

Travel opportunities

Office in Hellerup

Job summary

Ascendis Pharma is seeking an experienced Associate Project Director to lead GRAPS Enablement & Insights within Global Regulatory Affairs & Patient Safety. You will translate priorities into integrated plans, oversee cross-functional programs, and drive governance, reporting, and risk management across functions, geographies, and partners.

You will report to the GRAPS leadership team and may base in US or DK, with travel to Ascendis locations.

Qualifications

• At least 8 years in pharma/biotech or highly regulated industry.

Responsibilities

• Lead GRAPS projects from initiation to closeout with scope, milestones, budgets.
• Translate priorities into roadmaps and integrated plans.
• Create executive dashboards and concise decision materials.
• Coordinate multiple functions, geographies, vendors, and systems.
• Ensure quality, compliance, and inspection readiness.

Skills

Project management

Cross-functional leadership

Regulatory affairs

Pharma industry knowledge

Agile methods

Executive dashboards

Vendor management

GxP compliance

Education

Life sciences degree

Tools

Microsoft 365

MS Project

Job description

Ascendis Pharma is seeking an experienced Associate Project Director to lead GRAPS Enablement & Insights within Global Regulatory Affairs & Patient Safety. You will translate priorities into integrated plans, oversee cross-functional programs, and drive governance, reporting, and risk management across functions, geographies, and partners.

You will report to the GRAPS leadership team and may base in US or DK, with travel to Ascendis locations.